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rs1057519607

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057519607(-;C)
Make rs1057519607(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position18178849
GeneMYO15A
is asnp
is mentioned by
dbSNPrs1057519607
dbSNP (old)rs1057519607
ClinGenrs1057519607
ebirs1057519607
HLIrs1057519607
Exacrs1057519607
Gnomadrs1057519607
Varsomers1057519607
Maprs1057519607
PheGenIrs1057519607
Biobankrs1057519607
1000 genomesrs1057519607
hgdprs1057519607
ensemblrs1057519607
gopubmedrs1057519607
geneviewrs1057519607
scholarrs1057519607
googlers1057519607
pharmgkbrs1057519607
gwascentralrs1057519607
openSNPrs1057519607
23andMers1057519607
23andMe allrs1057519607
SNPshotrs1057519607
SNPdbers1057519607
MSV3drs1057519607
GWAS Ctlgrs1057519607
Max Magnitude0
ClinVar
Risk rs1057519607(C;C)
Alt rs1057519607(C;C)
Reference Rs1057519607(-;-)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18082163dupC
CLNSRC
CLNACC RCV000417125.1,